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Devon

FDA UDI

Class II (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Devon FDA UDI
Generic Name
Surgical drape clip, reusable FDA UDI
Device Name
Circumcision Clamp,Disposable FDA UDI
Model / Reference
56423 FDA UDI
Description
Circumcision Clamp,Disposable FDA UDI

Identifiers

Catalog Number
56423 FDA UDI
Primary DI / UDI-DI
20884527023070 FDA UDI
510(k) Number
K040052 FDA UDI
FDA Product Code
HFX FDA UDI
GMDN Term
Surgical drape clip, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.4530 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 1.3 Centimeter FDA UDI

Devon by Cardinalhealth — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

K040052 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI 9225cb86-280f-4698-a5a7-1e5d3e45693d 39 fields · synced Jun 8, 2026